Reported Nov 19, 2025 · Ongoing
BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
Becton Dickinson & Co.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212
Is this the product you have?
- BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
- Lot codes and dates
- Catalog No.: 246100
- UDI-DI30382902461006
- Lot Number
LM245590LM245592LM245593LM245594LM245666
- Amount recalled
- 29,760 units
Where it was sold
Why it was recalled
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.
This product could cause temporary or reversible health problems — stop using it.
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